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Measurement of the acute inflammatory response to walking exercise in COPD: effects of pulmonary rehabilitation

OBJECTIVE: This pilot study concerns the evaluation of the acute cytokine response to exercise and changes in this throughout a 7 week pulmonary rehabilitation programme. METHODS: 17 (10 male, 7 female) stable COPD patients, mean (SD) age 69 (8) yrs, mean FEV(1), 51.3 (17.3) % predicted entered into...

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Detalles Bibliográficos
Autores principales: Canavan, Jane, Garrod, Rachel, Marshall, Johanna, Jackson, David, Ansley, Paula, Jewell, Andy
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2695196/
https://www.ncbi.nlm.nih.gov/pubmed/18229573
Descripción
Sumario:OBJECTIVE: This pilot study concerns the evaluation of the acute cytokine response to exercise and changes in this throughout a 7 week pulmonary rehabilitation programme. METHODS: 17 (10 male, 7 female) stable COPD patients, mean (SD) age 69 (8) yrs, mean FEV(1), 51.3 (17.3) % predicted entered into 7 weeks of rehabilitation. The acute cytokine response (ACR) was measured from serum cytokine levels; Interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α) and C-reactive protein (CRP) taken pre, post and 1 hour post-maximal incremental shuttle walking test (ISWT). The ACR to maximal exercise was determined before rehabilitation (T0) and post rehabilitation (T7). The ACR (pre/post test) to iso-distance exercise (based on initial ISWT distance) was determined throughout the rehabilitation period at 2 (T2), 4 (T4) weeks and at the end (T7). RESULTS: 12 patients completed the study. Maximal ISWT distance significantly increased after rehabilitation. There was no significant change in baseline cytokine level throughout; or in pre/post-exercise cytokine levels prior to, during or following rehabilitation. CONCLUSIONS: There was no significant inflammatory response associated with maximal exercise before or after training. Cytokine responses to a fixed bout of exercise did not alter markedly throughout. Clinical PR is unlikely to exacerbate systemic inflammation in COPD.